Cholestyramine NDC 70771-1070

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1070Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1070Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70771-1070-1	70771107001	231 g in 1 CONTAINER (70771-1070-1)Marketed from Jun 8, 2017
70771-1070-2	70771107002	60 POUCH in 1 CARTON (70771-1070-2) / 5.5 g in 1 POUCHMarketed from Jun 8, 2017

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Cholestyramine
Generic name (nonproprietary): cholestyramine
Active ingredients: Cholestyramine — 4 g/5.5g
Dosage form: Powder, For suspension
Route: Oral
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202902
Marketing start: Jun 8, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Bile-acid Binding Activity (Mechanism)
Identifiers: Product ID 70771-1070_ec302f18-f250-422e-af1d-573743a0ce45SPL ID ec302f18-f250-422e-af1d-573743a0ce45SPL set ID d7c6bc5e-1916-43bf-b943-98f00f41b8deRxCUI 1801279UNII 4B33BGI082
Pharmacologic class: Bile Acid Sequestrant

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470771107001 followed by a unit qualifier and the quantity

Package 70771-1070-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 25, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE 1) Cholestyramine for oral suspension USP light powder, is indicated as adjunctive therapy to diet for the reduction of elevated serum cholesterol in patients with primary hypercholesterolemia (elevated low density lipoprotein [LDL] cholesterol) who do not respond adequately to diet. Cholestyramine for oral suspension USP light powder may be useful to lower LDL cholesterol in patients who also have hypertriglyceridemia, but it is not indicated where hypertriglyceridemia is the abnormality of most concern. Therapy with lipid-altering agents should be a component of multiple risk factor intervention in those individuals at significantly increased risk for atherosclerotic …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 202902

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 202902
Product	Strength	Form · route	Labeler	Product NDC
Cholestyramine	Cholestyramine 4 g/5.5g	Powder, For suspensionOral	Zydus Pharmaceuticals (USA) Inc.	68382-529